Guest guest Posted December 6, 2009 Report Share Posted December 6, 2009 Thanks for your reply. I'll be sure to get everything checked out to be safe, but as you say, it's likely just hemerroids or the endo on my bowels. I have not yet gone over with the surgeon all that he saw in there so will have a better idea Wednesday what's going on as far as the endo and where it was located. I too was depressed for a long time from the chronic pain. Effexor helped me a lot, and I also went to talk therapy. Did both for about a year, maybe a bit longer. I had a lot of unresolved emotional issues that actually had a big impact on my health. I'm in the best health I have been in years now, the sad part is that is still not very good, but I'm optimistic of things continuing to improve. I hope that you will be able to get the anxiety attacks under control, they are very scary when they happen. Betsy ________________________________ To: Hugs-N-Pain Sent: Sat, December 5, 2009 10:20:27 AM Subject: Re: Don't Be Too Shy to Talk to your Doctor... Hi, If you have a constipation problem, you likely just have hemorrhoids and the doc can easily tell that. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 8, 2009 Report Share Posted December 8, 2009 The constipation was from the surgery (lap for endometriosis) and has since resolved itself. I'm not generally on narcotics. Plan to get the other checked out soon as I'm healed up from the surgery. Not something to play with. I've been out of it the past few days so sorry for not responding sooner. Thanks for your reply. I'm sorry to hear about your depression, it is depressing to be sick all the time as you say. Sometimes it helps to talk to someone about it. I went to therapy for awhile (and was on an antidepressant) and it helped me a lot. I really think there is a link between depression and chronic pain, it's amazing how much better I've gotten since dealing with the depression. As you say, it gets stuck in a cycle. For me there will probably always be some sort of issues going on with my health, it just helps to have better coping strategies and a more positive outlook in spite of it. I'm rambling... Betsy ________________________________ To: Hugs-N-Pain Sent: Sat, December 5, 2009 1:07:01 PM Subject: Re: Don't Be Too Shy to Talk to your Doctor... > > > Hi, > If you have a constipation problem, you likely just have hemorrhoids and the doc can easily tell that. don't know your age, but a colonoscopy is recommended at age 50 then every 10 yrs after ... unless you have polyps the first one then they want to do every 3 year. I had one and they found 3 of them polyps, which tested precancerous so good thing i went in and had one. While the colonoscopy itself is done normally when you are sleeping, the prep for it is nasty. the nite before you gradually go off foods while drinking a gallon of " elephant laxative " so you are nice and clean when you go in for the procedure. I felt tired and weak by morning ugh! But when they do it, the thing they use actually opens up and snips off any polyps then brings them out for tests. I will take the colonoscopy anytime over colon cancer (who wants to wear a bag?). > > Guess from your post you also have chronic pain issues and take narcotics. The constipation from those can cause those piles easily but there are things you can do to keep from having those rock hard stools. Like eating a bowl of fiber cereal or oatmeal everyday for one. And there are " stool softeners " like the dulcolax one that are not laxatives, just soften the stool. the docs are supposed to counsel you about that before handing out narcs ya know? I have been on narcs for years, mostly like vicodin, for DDD in my neck, arthritis and stuff in spine. I get them to switch the med now and then to try to avoid being too addicted. Have had darvocettes, also ty-3's, but they have not wanted to give me anything stronger yet. I have pain everyday, and have since 1991 when i got an ankle/foot fracture while in Navy. Someone karate kicked my ankle at that joint on the outside and shattered my left fib into like 50 pieces. Since the surgery i have arthritis in there pretty good (they dont tell you about that beforehand) but the DDD and stuff hurts far worse. > > Anyways, good luck with your recovery, you right that was a long post lol. And also with your pain issues. I became depressed clinically from my chronic pain, and while that has become better, it has 'morphed' into anxiety attacks severe enough that i am now on disability. I always tell them docs that the vicious circles of chronic pain and depression/anxiety disorders touch somewhere; they actually feed off each other. So I take effexor for my MH stuff, also have a " pam " i.e. valium like (serax) for anxiety attacks, ty3 right now for pain too, and metoprolol for a heart rate issue caused by my panic attacks (fast enough to be dangerous without). > > Happy Holidays to all (and maybe a white xmas too) > chris in Indy > > ps-i recently joined here, so dont know everyones story, i am on groups for my anxiety and stuff, also a DDD group for my spine issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 8, 2009 Report Share Posted December 8, 2009 , thanks... don't worry, I wouldn't take medical advice off the internet! My health is way more important than that *smiles* I did mention the problem to my Dr. and he was the one that suggested the possibility of a hemorroid (because of rectal bleeding off and on). He also stressed that it is important for me to follow up with a specialist and get checked out further in case it should be something more serious. Betsy > Betsy that post was wrong even though the only way a hemorrhoid causes constipation is if its large enough and then you would probably feel it and it would be an internal hemorrhoid. But what you may want to do is just take a laxative and see what happens. But if your worried about I'd call your doctor I wouldn't listen to any medical advice given in an online support group. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 8, 2009 Report Share Posted December 8, 2009 That depression is pretty normal.  Think of the five stages of grief.  We seem to cycle thru those layers over and over.  It's grief for the loss of your body and what you use to do.  It helps when you can replace what you used to do with something else equally enjoying.  I know playing with T Shirt shops and staying busy on the computer really helps that problem.  As long as I can do something.  And that keeps me busy all day every day and it fun. I still miss being able to move without paying dearly for it for the next three or four days....like cooking Thanksgiving dinner.  I paid like a sonofagun!!  For days after I hurt like hell. At any rate...those losses really can get to you and most folks don't realize it's that normal stages of grief.  http://en.wikipedia.org/wiki/K%C3%BCbler-Ross_model In chronic pain...http://www.liebertonline.com/doi/abs/10.1089/act.1998.4.231 Lotacats “I love cats because I enjoy my home; and little by little, they become its visible soul.†Twitter_follow me http://twitter.com/LotacatsFunPix Express Chronic Pain Awareness http://www.cafepress.com/lotacatspix/5815010 Lotacatsfunpix.com http://www.lotacatsfunpix.com/ Deviantart http://lotacats05.deviantart.com/ Subject: Re: Re: Don't Be Too Shy to Talk to your Doctor... To: Hugs-N-Pain Date: Tuesday, December 8, 2009, 7:25 AM  The constipation was from the surgery (lap for endometriosis) and has since resolved itself. I'm not generally on narcotics. Plan to get the other checked out soon as I'm healed up from the surgery. Not something to play with. I've been out of it the past few days so sorry for not responding sooner. Thanks for your reply. I'm sorry to hear about your depression, it is depressing to be sick all the time as you say. Sometimes it helps to talk to someone about it. I went to therapy for awhile (and was on an antidepressant) and it helped me a lot. I really think there is a link between depression and chronic pain, it's amazing how much better I've gotten since dealing with the depression. As you say, it gets stuck in a cycle. For me there will probably always be some sort of issues going on with my health, it just helps to have better coping strategies and a more positive outlook in spite of it. I'm rambling... Betsy ____________ _________ _________ __ From: " melis-aatt (DOT) net " <melis-aatt (DOT) net> To: Hugs-N-Pain@ yahoogroups. com Sent: Sat, December 5, 2009 1:07:01 PM Subject: Re: Don't Be Too Shy to Talk to your Doctor... > > > Hi, > If you have a constipation problem, you likely just have hemorrhoids and the doc can easily tell that. don't know your age, but a colonoscopy is recommended at age 50 then every 10 yrs after ... unless you have polyps the first one then they want to do every 3 year. I had one and they found 3 of them polyps, which tested precancerous so good thing i went in and had one. While the colonoscopy itself is done normally when you are sleeping, the prep for it is nasty. the nite before you gradually go off foods while drinking a gallon of " elephant laxative " so you are nice and clean when you go in for the procedure. I felt tired and weak by morning ugh! But when they do it, the thing they use actually opens up and snips off any polyps then brings them out for tests. I will take the colonoscopy anytime over colon cancer (who wants to wear a bag?). > > Guess from your post you also have chronic pain issues and take narcotics. The constipation from those can cause those piles easily but there are things you can do to keep from having those rock hard stools. Like eating a bowl of fiber cereal or oatmeal everyday for one. And there are " stool softeners " like the dulcolax one that are not laxatives, just soften the stool. the docs are supposed to counsel you about that before handing out narcs ya know? I have been on narcs for years, mostly like vicodin, for DDD in my neck, arthritis and stuff in spine. I get them to switch the med now and then to try to avoid being too addicted. Have had darvocettes, also ty-3's, but they have not wanted to give me anything stronger yet. I have pain everyday, and have since 1991 when i got an ankle/foot fracture while in Navy. Someone karate kicked my ankle at that joint on the outside and shattered my left fib into like 50 pieces. Since the surgery i have arthritis in there pretty good (they dont tell you about that beforehand) but the DDD and stuff hurts far worse. > > Anyways, good luck with your recovery, you right that was a long post lol. And also with your pain issues. I became depressed clinically from my chronic pain, and while that has become better, it has 'morphed' into anxiety attacks severe enough that i am now on disability. I always tell them docs that the vicious circles of chronic pain and depression/anxiety disorders touch somewhere; they actually feed off each other. So I take effexor for my MH stuff, also have a " pam " i.e. valium like (serax) for anxiety attacks, ty3 right now for pain too, and metoprolol for a heart rate issue caused by my panic attacks (fast enough to be dangerous without). > > Happy Holidays to all (and maybe a white xmas too) > chris in Indy > > ps-i recently joined here, so dont know everyones story, i am on groups for my anxiety and stuff, also a DDD group for my spine issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2009 Report Share Posted December 11, 2009 Right now it's four cats....one seems to have a touch of ADD so it seems like more. I've had more. I have fibromyalgia/myofacial pain sydrome. I have had Osteoarthritis since my 20's and I'm 67 or around there...I stopped checking. lol....born 1942. So the Osteo is really full throttle now and I have advanced, debilitating osteoarthtitis. It manage to munch thru the L3 and L4 vertibrea and cause nerve damage so I have RSD symptoms in my left leg. Burning, stinging, numbness and so on...super sinsitive skin. That's why we were trying to gabapentine. Won't work for me. I'm on MsContin 30mg twice a day, Tyl. #3's for breakthru pain. Thyroid cause my gland is removed and ranitidine for heartburn, gurd type of junk. I tolerate all of those drugs very well...except the gabapentine. Awful...ad won't work. Gonna have to live with burning. I'm super gimpy but I have my computer which I tolerate sitting at all day.....thank Heavens. I do several T Shirt shops online and doing the pictures by mouse drawing I keep busy and the day goes fast. I do some volunteer work for an online safety and education outfit that helps internet victims of harassments/stalking and such. That keeps me out of trouble as well. I love computers. I absolutely fear not having one. I learned to build them from scratch and fix them as much as possible for a self taught 'puter person. I'm in the process of building a new one to back up this one...I aslo built. I have a very old one that the techs said was dead and needed burial but I found the old style motherboards on a site that sells them and replaced it and it works fine now. I love that kind of challenge. That's about it and my life as it is. My son and I share an apartment big enough to respect each others space and he helps me with getting to the doctor and such. The pain makes it too difficult to drive anywhere except very local...as in a few blocks. Shouldn't drive with the MsContin anyway. He has a twin currently serving in Afghanistan...now home for a couple of weeks. Those jerks make two weeks of their leave in travel time. So he gets only two weeks at home. That sux. When he was in the army stryker brigade that wasn't the case. They got the whole month at home. When he was discharged he joined the Nev National Guards and that's why he's on his 2nd deployment.   I have another son in Washington...I'm down in Nevada....but we communicate a lot on weekends via the IM. That's my life as it is in the nut shell. My cats keep my sanity as well. One is a rescue catm Marshall and just about the brightest cat I've ever known. He's a prize. Then there's my mean cat, CC and my schizo cat Gizmo and the clown of the bunch, Byte. He screws with the others...except Marshall. Lotacats “I love cats because I enjoy my home; and little by little, they become its visible soul.†Twitter_follow me http://twitter.com/LotacatsFunPix Express Chronic Pain Awareness http://www.cafepress.com/lotacatspix/5815010 Lotacatsfunpix.com http://www.lotacatsfunpix.com/ Deviantart http://lotacats05.deviantart.com/ Subject: Re: Don't Be Too Shy to Talk to your Doctor... To: Hugs-N-Pain Date: Friday, December 11, 2009, 7:31 AM  hi, how many cats are a " lotacats? " i have a colony of ferals/abandoned pets that I care for. They are about a baker's dozen most of the time. We have something called " TNR " here, for Trap/Neuter/ Return (or Release lol) an alternative to the animal control catching them and putting them to sleep. So a local org. called Indyferal helps with the trapping and stuff, they come back with the left ear " ear-tipped " so animal control knows the kitties are in a " managed colony " and not to bother them. They all get fixed too which helps. The cats are quieter, no spraying lots less fights. I have had some since 2001 when I started with 4. Just lost one of those to likely FeLk which is bad. Hope none of the rest get it. Got some pet kitties and inbetweens too so lotsa cats here lol. have battled depression on and off since 1991 when I was in first gulf war. also have anxiety issues that have caused panic attacks. the depression has responded much better to the meds than the anxiety ... i am on disability for that and physical issues like my DDD in neck. Nerve to right arm is pinched bad enough to mess up my arm it falls alsleep when i do much and was a financial type before. Cant sit at the puter all day now. Since over 50 SS says I can have the SSDI. VA gives me money too for my service connected stuff (the anxiety/depression and stuff). don't know what your conditions are, just joined not long ago but we both like kitties. happy holidays, chris in IN > > That depression is pretty normal.  Think of the five stages of grief.  We seem to cycle thru those layers over and over.  It's grief for the loss of your body and what you use to do.  It helps when you can replace what you used to do with something else equally enjoying.  I know playing with T Shirt shops and staying busy on the computer really helps that problem.  As long as I can do something.  And that keeps me busy all day every day and it fun. > I still miss being able to move without paying dearly for it for the next three or four days....like cooking Thanksgiving dinner.  I paid like a sonofagun!!  For days after I hurt like hell. > At any rate...those losses really can get to you and most folks don't realize it's that normal stages of grief.  > http://en.wikipedia .org/wiki/ K%C3%BCbler- Ross_model > In chronic pain...http: //www.liebertonl ine.com/doi/ abs/10.1089/ act..1998. 4.231 > > Lotacats > > > > “I love cats because I enjoy my home; and little by little, they become its visible soul.†> > > > Twitter_follow me > > http://twitter. com/LotacatsFunP ix > > > > Express Chronic Pain Awareness > > http://www.cafepres s.com/lotacatspi x/5815010 > > > > Lotacatsfunpix. com > > http://www.lotacats funpix.com/ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2009 Report Share Posted December 11, 2009 in IN Re: 1st gulf war OT Our son that is 55 now was in the first gulf war. Lots of stories if I can get him in the mood to talk about them. He divorced after getting home and now is happily married and lives in Denver. I wish you luck with your depression. Luckily he came out of it ok for the most part. He was stationed at Fort , Kentucky when he retired out of the service. Lois > Right now it's four cats....one seems to have a touch of ADD so it seems > like more. I've had more. > > I have fibromyalgia/myofacial pain sydrome. I have had Osteoarthritis since > my 20's and I'm 67 or around there...I stopped checking. lol....born 1942. > > So the Osteo is really full throttle now and I have advanced, debilitating > osteoarthtitis. It manage to munch thru the L3 and L4 vertibrea and cause > nerve damage so I have RSD symptoms in my left leg. Burning, stinging, > numbness and so on...super sinsitive skin. That's why we were trying to > gabapentine. Won't work for me. I'm on MsContin 30mg twice a day, Tyl. > #3's for breakthru pain. Thyroid cause my gland is removed and ranitidine > for heartburn, gurd type of junk. I tolerate all of those drugs very > well...except the gabapentine. Awful...ad won't work. Gonna have to live > with burning. > > I'm super gimpy but I have my computer which I tolerate sitting at all > day.....thank Heavens. I do several T Shirt shops online and doing the > pictures by mouse drawing I keep busy and the day goes fast. I do some > volunteer work for an online safety and education outfit that helps internet > victims of harassments/stalking and such. That keeps me out of trouble as > well. > > I love computers. I absolutely fear not having one. I learned to build them > from scratch and fix them as much as possible for a self taught 'puter > person. I'm in the process of building a new one to back up this one...I > aslo built. I have a very old one that the techs said was dead and needed > burial but I found the old style motherboards on a site that sells them and > replaced it and it works fine now. I love that kind of challenge. > > That's about it and my life as it is. My son and I share an apartment big > enough to respect each others space and he helps me with getting to the > doctor and such. The pain makes it too difficult to drive anywhere except > very local...as in a few blocks. Shouldn't drive with the MsContin anyway. > > He has a twin currently serving in Afghanistan...now home for a couple of > weeks. Those jerks make two weeks of their leave in travel time. So he > gets only two weeks at home. That sux. When he was in the army stryker > brigade that wasn't the case. They got the whole month at home. When he > was discharged he joined the Nev National Guards and that's why he's on his > 2nd deployment. I have another son in Washington...I'm down in > Nevada....but we communicate a lot on weekends via the IM. > > That's my life as it is in the nut shell. My cats keep my sanity as well. > One is a rescue catm Marshall and just about the brightest cat I've ever > known. He's a prize. Then there's my mean cat, CC and my schizo cat Gizmo > and the clown of the bunch, Byte. He screws with the others...except > Marshall. > > Lotacats > > > > “I love cats because I enjoy my home; and little by little, they become its > visible soul.” > > > > Twitter_follow me > > http://twitter.com/LotacatsFunPix > > > > Express Chronic Pain Awareness > > http://www.cafepress.com/lotacatspix/5815010 > > > > Lotacatsfunpix.com > > http://www.lotacatsfunpix.com/ > > > > Deviantart > > http://lotacats05.deviantart.com/ > > > > > Subject: Re: Don't Be Too Shy to Talk to your Doctor... > To: Hugs-N-Pain > Date: Friday, December 11, 2009, 7:31 AM > > > > > > > > > > > > > > > > > > > > hi, > > how many cats are a " lotacats? " i have a colony of ferals/abandoned > pets that I care for. They are about a baker's dozen most of the time. We > have something called " TNR " here, for Trap/Neuter/ Return (or Release lol) > an alternative to the animal control catching them and putting them to > sleep. So a local org. called Indyferal helps with the trapping and stuff, > they come back with the left ear " ear-tipped " so animal control knows the > kitties are in a " managed colony " and not to bother them. They all get > fixed too which helps. The cats are quieter, no spraying lots less fights. > I have had some since 2001 when I started with 4. Just lost one of those to > likely FeLk which is bad. Hope none of the rest get it. Got some pet > kitties and inbetweens too so lotsa cats here lol. > > > > have battled depression on and off since 1991 when I was in first gulf war. > also have anxiety issues that have caused panic attacks. the depression has > responded much better to the meds than the anxiety ... i am on disability > for that and physical issues like my DDD in neck. Nerve to right arm is > pinched bad enough to mess up my arm it falls alsleep when i do much and was > a financial type before. Cant sit at the puter all day now. Since over 50 > SS says I can have the SSDI. VA gives me money too for my service connected > stuff (the anxiety/depression and stuff). don't know what your conditions > are, just joined not long ago but we both like kitties. > > > > happy holidays, > > chris in IN > > > > > >> > >> That depression is pretty normal. Think of the five stages of grief. We >> seem to cycle thru those layers over and over. It's grief for the loss of >> your body and what you use to do. It helps when you can replace what you >> used to do with something else equally enjoying. I know playing with T >> Shirt shops and staying busy on the computer really helps that problem. >> As long as I can do something. And that keeps me busy all day every day >> and it fun. > >> I still miss being able to move without paying dearly for it for the next >> three or four days....like cooking Thanksgiving dinner. I paid like a >> sonofagun!! For days after I hurt like hell. > >> At any rate...those losses really can get to you and most folks don't >> realize it's that normal stages of grief. > >> http://en.wikipedia .org/wiki/ K%C3%BCbler- Ross_model > >> In chronic pain...http: //www.liebertonl ine.com/doi/ abs/10.1089/ >> act..1998. 4.231 > >> > >> Lotacats > >> > >> > >> > >> “I love cats because I enjoy my home; and little by little, they become >> its visible soul.” > >> > >> > >> > >> Twitter_follow me > >> > >> http://twitter. com/LotacatsFunP ix > >> > >> > >> > >> Express Chronic Pain Awareness > >> > >> http://www.cafepres s.com/lotacatspi x/5815010 > >> > >> > >> > >> Lotacatsfunpix. com > >> > >> http://www.lotacats funpix.com/ > >> > >> > >> > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2009 Report Share Posted December 13, 2009 I have cats also several outdoors and 2 indoors My pets is what helps me get up in the morning If not for them I would be more content to spend the day in bed Wanda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2009 Report Share Posted December 17, 2009 hi Wanda, Me too.  If it weren't for our 2 cats I would be the same way. They motivate me to get out of bed and hobble outside and make sure they have food and water. They love the attention and I love to give it to them. I have to have some sort of pet. I just adore cats. I adore dogs as well but am not able to walk them and we have no place for a fenced in yard.  Cats are good that way, they know where their home is and they come when I call them to feed them. I usually feed just dry food with a few of those cat treats during the day but at night as it is colder I give them a little bit of canned cat food. I mix it with their dry food. I use picker uppers so I don't have to bend down to give them their food dish. Our cats also jump up on the railing outside to be petted so I don't have to bend over. Works out pretty well. I just wish my fiancee didn't have such allergies so the cats could come inside if they wanted to. They do just find outside, they love to hunt and climb the trees. I could not live without a pet. I love them so much. hugs, Coleen ps. wish me luck Friday as I have a bit of walking to do again. We have to go to my fiancee's Ear, Nose and Throat doctor to see if they can help him with his sinus problems. First we are going to Walmart. Now that I have a few extra pounds on me I really hurt bad when I try to walk a bit. I couldn't carry the extra weight that I gained in my arms in the first place and now I have to because it is in my body. ouch! I really hope they have those handicap carts available. I will lose these few pounds as I couldn't even carry them before in a bag! lol I forgot how fattening peanut butter was! lol ________________________________ To: Hugs-N-Pain Sent: Sun, December 13, 2009 8:28:56 PM Subject: Re: Re: Don't Be Too Shy to Talk to your Doctor...  I have cats also several outdoors and 2 indoors My pets is what helps me get up in the morning If not for them I would be more content to spend the day in bed Wanda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2009 Report Share Posted December 18, 2009 Coleen How are you feeling after all the walking today Did they have the carts available to ride Wanda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2009 Report Share Posted December 21, 2009 I agree about the water aerobics. They are a life saver! Most exercise makes my pain much worse, but after an hour of jumping around in the water, I feel great. It is also a great place to meet people with physical disabilities who are in the same boat as you are. I try to go 3 to 4 times a week. Where there's a will there's a way! Hugs, Alanna Sent from my Verizon Wireless BlackBerry Re: Re: Don't Be Too Shy to Talk to your Doctor... > > Â > I have cats also several outdoors and 2 indoors > My pets is what helps me get up in the morning > If not for them I would be more content to spend the day in bed > > Wanda > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2009 Report Share Posted December 21, 2009 Hello been up since 9pm it is now 2 am I have a question and would prefer allot of feed back. I have to staart today with a NEW PCP he does not know my history and my pain clinic ( which I am leaving ) refuses pain meds. thye want it dont strickly by my PCP. I need to know, what to ask how to ask and the most vital subjects I should go over with him tomorrow. I dont want to go in there and just say I need pain meds too. I am sick of being looked at as an addict.Please Id be grateful for any help. my appointment is at 1:30 today www.reaganroundup.comhttp://groups.yahoo.com/group/lenaweeplanttraders/ Subject: Re: Re: Don't Be Too Shy to Talk to your Doctor... To: Hugs-N-Pain Date: Monday, December 21, 2009, 9:33 AM I agree about the water aerobics. They are a life saver! Most exercise makes my pain much worse, but after an hour of jumping around in the water, I feel great. It is also a great place to meet people with physical disabilities who are in the same boat as you are. I try to go 3 to 4 times a week. Where there's a will there's a way! Hugs, Alanna Sent from my Verizon Wireless BlackBerry Re: Re: Don't Be Too Shy to Talk to your Doctor... > > > I have cats also several outdoors and 2 indoors > My pets is what helps me get up in the morning > If not for them I would be more content to spend the day in bed > > Wanda > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2009 Report Share Posted December 22, 2009 I do not have direct medical records but I do have all my MRI reports and disk. www.reaganroundup.comhttp://groups.yahoo.com/group/lenaweeplanttraders/ Subject: Re: Don't Be Too Shy to Talk to your Doctor... To: Hugs-N-Pain Date: Tuesday, December 22, 2009, 5:16 AM Â n, Good luck with your appt. If you have any copies of your medical records be sure to take some in with you. Then he will know you are not faking just to get pain meds. Just be advised that some PCP's DO NOT prescribe narcotics... period. I am sort of in the same boat with the VA system. The PCP is in charge of prescribing my pain meds. In the years that I have been going there it probably took several years to convince her I was in enough pain to warrant anything stronger than naproxen or ibuprofen. She has prescribed me darvocette, vicodin, and ty3's over the past few yrs, but has refused to prescribe any long acting stuff (like the patch which i have asked for, or stronger meds). This past year I got approved for SSDI and Medicare. I decided to consult an " outside " doctor and went to one who specialized in Internal Medicine. He told me " I don't believe in prescribing any narcotics " then " do you want some naproxin? " I said " Why? It does not do anything. " And have not been back to see him tho I may try again this coming year to see about getting a recommendation to the Pain Clinic at the Hospital or maybe a neuro consult or both. My Medicare plan is going to be with an HMO Advantage Plan this coming year so have to go thru the PCP to go anyplace else, sort of like the VA. Keep us posted on how it went... good luck and happy holidays, chris in IN > > Hello been up since 9pm it is now 2 am I have a question and would prefer allot of feed back. I have to staart today with a NEW PCP he does not know my history and my pain clinic ( which I am leaving ) refuses pain meds. thye want it dont strickly by my PCP. I need to know, what to ask how to ask and the most vital subjects I should go over with him tomorrow. I dont want to go in there and just say I need pain meds too. I am sick of being looked at as an addict.Please Id be grateful for any help. my appointment is at 1:30 today > > > www.reaganroundup. comhttp:/ /groups.yahoo. com/group/ lenaweeplanttrad ers/ > Quote Link to comment Share on other sites More sharing options...
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